FDA 510(k) Applications Submitted by VUNO Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K231398 05/15/2023 VUNO Med-DeepBrain VUNO Inc.
K241439 05/21/2024 VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage Vuno Inc.


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